At Ribocure, we are driven by science and innovation, with a mission to establish a world-leading company in RNA research and development, ultimately making a positive impact on patients worldwide. We are seeking a Clinical Program Director to join our growing Clinical Operations team and take a leadership role in driving the successful execution of our clinical programs.

In this role, you will lead clinical programs across all phases of development, driving the strategic development of the Clinical Development Plan (CDP) and ensuring delivering of high-quality clinical trials. You will manage cross-functional teams, coordinate with internal stakeholders and external partners, and oversee all aspects of clinical trial operations, including trial planning, execution, risk management and vendor oversight.

We are looking for a candidate with experience in clinical program leadership in the pharmaceutical/biotech industry, strong leadership skills, and the ability to combine strategic vision with hands-on execution in a fast-paced, innovative environment.

Key responsibilities:

• Lead the Clinical Project Team (CPT) and operational trial teams, driving program strategy, trial design, and the delivery of clinical trials in line with the clinical development plan.
• Provide program leadership and direction to ensure adherence to scope, quality, budget, timelines, and proactive risk management; escalate key program issues to the Global Project Team (GPT).
• Establish and develop high-performing teams, ensuring Clinical Operations expertise and active cross-functional collaboration (e.g., Medical, Clinical Pharmacology, Regulatory, Biostatistics) to support program and trial activities.
• Lead/oversee planning, start-up, conduct, reporting, and close-out of clinical trials, ensuring compliance with regulatory requirements, GCP/ICH, and industry standards.
• Drive development and maintenance of key trial documents and operational plans; contribute to protocols, applications, and regulatory submissions in collaboration with relevant functions.

• Build and maintain strong relationships with investigators, clinical sites, and key opinion leaders (KOLs) within the program area, ensuring effective engagement and scientific/operational alignment.
• Manage external partners, including CROs and vendors: vendor selection, contracting, oversight, and performance management to ensure quality, cost, and timely delivery.

Requirements:

• University degree, preferably in medical or biological science or discipline associated with clinical research
• At least 7 years’ experience from within the pharmaceutical industry and proven experience of clinical development / drug development process in various phases of development and therapy areas
• Comprehensive knowledge of the clinical and pharmaceutical drug development process
• Excellent knowledge of ICH-GCP principles
• Strong organizational skills and ability to manage multiple priorities
• Excellent communication and organizational skills

Desired requirements:

• Experience in managing early clinical trials
• Project management certification

Why Join Us?

We offer more than a job – we offer a mission. You’ll be part of a tight-knit, friendly team working on real challenges with real potential. Your ideas matter. Your work matters. And your growth matters to us.

Ready to Apply?

We encourage you to submit your CV and cover letter promptly, as applications will be reviewed on an ongoing basis. Final application deadline: October 10.

Hiring manager: Rebeckha Magnusson, Head of Clinical Operations & QA

This recruitment is quality assured by HR On Demand.